Epilepsy genetics — past, present, and future

This publication has 76 references indexed in Scilit:

• A map of human genome variation from population-scale sequencing
  Nature, 2010
• A Focal Epilepsy and Intellectual Disability Syndrome Is Due to a Mutation in TBC1D24
  The American Journal of Human Genetics, 2010
• TBC1D24, an ARF6-Interacting Protein, Is Mutated in Familial Infantile Myoclonic Epilepsy
  The American Journal of Human Genetics, 2010
• Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study
  Brain, 2010
• Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes
  The American Journal of Human Genetics, 2010
• Mutations in PNKP cause microcephaly, seizures and defects in DNA repair
  Nature Genetics, 2010
• Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies
  Brain, 2009
• Genetics of complex neurological disease: challenges and opportunities for modeling epilepsy in mice and rats
  Trends in Genetics, 2009
• Targeted loss of Arx results in a developmental epilepsy mouse model and recapitulates the human phenotype in heterozygous females
  Brain, 2009
• X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment
  Nature Genetics, 2008